WO2018170238A2 - Methods and compositions for inducing immune responses against clostridium difficile - Google Patents

Methods and compositions for inducing immune responses against clostridium difficile Download PDF

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Publication number
WO2018170238A2
WO2018170238A2 PCT/US2018/022597 US2018022597W WO2018170238A2 WO 2018170238 A2 WO2018170238 A2 WO 2018170238A2 US 2018022597 W US2018022597 W US 2018022597W WO 2018170238 A2 WO2018170238 A2 WO 2018170238A2
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WIPO (PCT)
Prior art keywords
toxin
protein
amino acid
polypeptide
multivalent immunogenic
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PCT/US2018/022597
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English (en)
French (fr)
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WO2018170238A3 (en
Inventor
Jing-Hui Tian
Ye Liu
Gale Smith
Gregory Glenn
David Flyer
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Novavax, Inc.
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Priority to US16/494,517 priority Critical patent/US11123419B2/en
Priority to CA3056090A priority patent/CA3056090A1/en
Application filed by Novavax, Inc. filed Critical Novavax, Inc.
Priority to CN201880025192.8A priority patent/CN110691609B/zh
Priority to RU2019132111A priority patent/RU2781057C9/ru
Priority to JP2019550687A priority patent/JP7149285B2/ja
Priority to MX2019010948A priority patent/MX2019010948A/es
Priority to KR1020197030108A priority patent/KR102640722B1/ko
Priority to SG11201908376U priority patent/SG11201908376UA/en
Priority to AU2018236352A priority patent/AU2018236352B2/en
Priority to IL269258A priority patent/IL269258B2/en
Priority to EP18767173.0A priority patent/EP3595709A4/en
Priority to BR112019019117A priority patent/BR112019019117A2/pt
Publication of WO2018170238A2 publication Critical patent/WO2018170238A2/en
Publication of WO2018170238A3 publication Critical patent/WO2018170238A3/en
Priority to US17/398,610 priority patent/US11938179B2/en
Priority to JP2022153071A priority patent/JP7397145B2/ja

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/02—Bacterial antigens
    • A61K39/08—Clostridium, e.g. Clostridium tetani
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/02—Bacterial antigens
    • A61K39/116—Polyvalent bacterial antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
    • C07K14/33—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Clostridium (G)
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55505—Inorganic adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55577—Saponins; Quil A; QS21; ISCOMS
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/70—Multivalent vaccine
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2319/00—Fusion polypeptide
    • C07K2319/55—Fusion polypeptide containing a fusion with a toxin, e.g. diphteria toxin

Definitions

  • Vaccination against disease using a subunit-based vaccine is dependent on producing sufficient amounts of the protein antigen and maintaining stability of the antigen such that the protein remains effective when administered to a target population.
  • Target protein can be produced at low levels, or can be insoluble, resulting in economically- unfavorable production, even when the protein had particularly favorable immunogenicity profile.
  • Bacterial infections remain a health concern. Indeed, bacterial vaccines are increasingly sought after as bacteria evolve resistance to front-line antibiotics. Bacterial subunit vaccines rely on recombinant protein production. However, bacterial proteins can often be difficult to produce at high level due to low expression, and insolubility, and they can also suffer from reduced stability. Better approaches to producing vaccines, particularly for difficult antigen targets, would thus provide global health benefits.
  • infection by clostridial bacteria notably C. difficile remains a particular problem. Clostridium difficile infection (CDI) is the leading cause of nosocomial antibiotic-associated diarrhea in developed countries. Hypervirulent strains have evolved causing severe disease with increased mortality.
  • Homologous glucosylating toxins TcdA and TcdB, and binary ADP-ribosylating toxin (CDT) are major virulence factors causing pathogenesis. There is an unmet need for vaccines targeting these toxins.
  • compositions contain polypeptides containing multiple C. difficile toxins, which, when administered to a subject, induce advantageous immune responses.
  • Methods for producing the multi-toxin polypeptides are also disclosed.
  • Figure 1 C difficile triple toxin vaccine constructs.
  • Figure shows illustration of C.diff triple toxin vaccine containing the binding domains of CDTb, Ted B, and Ted A with (construct 1420) and without (construct 1470) a furin cleavage site after the activation domain of CDTb.
  • FIG. 1 Expression and solubility of triple toxin vaccine BV1470 and BV1420.
  • Spodoptera frugiperda Sf9 insect cells were infected at a MOI of 0.1 with recombinant baculovirus B VI 420 and B VI 470, harvested at 48 and 72 hours postinfection, and analyzed for protein expression by SDS-PAGE and coomassie staining.
  • An equal volume of total protein (T, cells and medium) and clarified medium (M) were mixed with 2X SDS-PAGE sample buffer and run on a 4%-12% polyacrilamide NuPage gel.
  • Figure 3 Time course expression of triple toxin vaccine BV1470 and BV1420.
  • FIG. 5 Purification of triple toxin vaccine BV1470 from Sf9 cells. Triple toxin vaccine BV1470 was purified from infected cells as described in Figure 8. Final filtered product from the Source 30Q column was analyzed for purity by SDS-PAGE and coomassie staining. Triple toxin protein was identified by western blot using anti-CDTb, anti-TcdB, and antiTcdA antibodies.
  • FIG. 6 Purification of triple toxin vaccine BV1420 from Sf9 cells. Triple toxin vaccine BV1420 was purified from infected cells as described in Figure 8. Final filtered product from the Source 30Q column was analyzed for purity by SDS-PAGE and coomassie staining. Triple toxin protein was identified by western blot using anti-TcdB antibodies.
  • FIG. 7 Particle size distribution by volume graph for triple toxin BV1420.
  • Particle size of triple toxin B VI 420 was determined by dynamic light scattering using a Zeta Sizer Nano. Graph of size distribution by volume is shown.
  • Figure 8 Particle size distribution by intensity graph for triple toxin BV1470.
  • Particle size of triple toxin BV1420 was determined by dynamic light scattering using a Zeta Sizer Nano. Graph of size distribution by intensity is shown.
  • FIGS 9A-9D Electronmicrographs of negative stained triple toxin BV1420.
  • Electron-micrograph of purified triple toxin BV1420 was diluted to approximately lOug/ml and negatively stained with uranyl acetate.
  • FIG. 10 BV1420 triple toxin vaccine mouse lethal toxin challenge study 1. Mice were immunized on day zero and day 14 with triple toxin vaccine BV1420 and challenged on day 35 with a lethal dose of Ted A or CDT and monitored for 10 days post challenge. Mice were bleed as shown and serum analyzed for anti-toxin IgG and for toxin neutralizing antibodies. Animals were monitored for mortality and morbidity for 10 days after toxin challenge. [0017] Figure 11. BV1420 triple toxin vaccine mouse lethal toxin challenge study 1 - serum anti-toxin IgG responses. Day 42 serum samples were assayed for Anti-Ted A, anti-Ted B, and anti-CDT IgG titers by ELISA using native toxins bound to plates.
  • FIG. 12 BV1420 triple toxin vaccine mouse lethal toxin challenge study 1 - toxin neutralizing antibody (TNA) titers. Toxin neutralization titers were determined using a colorimetric Vero cell based assay. Titer indicated are the reciprocal of the highest dilution of serum that did not kill cells.
  • TAA toxin neutralizing antibody
  • Figure 13 BV1420 triple toxin vaccine mouse lethal toxin challenge study 1 - animal survival. Animal survival was determined 10 days post challenge. Animals showing greater than 20% weight loss were sacrificed and recorded as dead.
  • FIG. 14 BV1420 triple toxin vaccine mouse lethal toxin challenge study 2 - toxin B survival. Mice were immunized on day zero and day 14 with triple toxin vaccine B VI 420 and challenged on day 35 with a lethal dose of Ted B and monitored for 10 days post challenge. Mice were bled as shown and serum analyzed for anti-toxin IgG and for toxin neutralizing antibodies (TNA). Animals were monitored for mortality and morbidity for 10 days after toxin challenge.
  • TAA toxin neutralizing antibodies
  • Figure 15 BV1420 triple toxin vaccine mouse lethal toxin challenge study 2 - antitoxin IgG levels. Day 42 serum samples were assayed for Anti-Ted A, anti-Ted B, and anti- CDT IgG titers by ELISA using native toxins bound to plates.
  • Figure 16 BV1420 triple toxin vaccine mouse lethal toxin challenge study 2 - toxin B TNA titers. Toxin neutralization titers were determined using a colorimetric Vero cell based assay. Titer indicated are the reciprocal of the highest dilution of serum that did not kill cells.
  • Figure 17 BV1420 triple toxin vaccine mouse lethal toxin challenge study 2 - toxin B survival. Animal survival was determined 10 days post challenge. Animals showing greater than 20% weight loss were sacrificed and recorded as dead.
  • FIG. 18 Additional vaccine proteins with the TcdB gene translocation domain are shown. BV1512 is shown in the bottom diagram.
  • FIG. 19 Multimer Protein Expression: Expression and western blot analysis of multimer protein BV 1512.
  • Figure 20 Quadrivalent Multimer Protein Expression:
  • Figure 25 illustrates two quadrivalent multimer proteins. In both cases, a peptide from a second TcdB strain is introduced to broaden immunity against multiple strains. In the upper diagram, the TcdB peptide from Strain 027 is added at the C-terminus. In the lower diagram, the peptide is introduced between the TcdB protein and the TcdA(R19) protein from the first strain, strain 630.
  • FIG. 21 Quadrivalent Multimer Protein Expression: Expression and western blot analysis of the quadrivalent protein shown in the upper diagram of Figure 20.
  • FIG. 22 Quadrivalent Multimer Protein Expression: Expression and western blot analysis of the quadrivalent protein shown in the lower diagram of Figure 20.
  • FIG 23 C difficile Toxins and Design of Chimeric Trivalent (T) and Quadravalent (Q) Toxin Fusion Proteins.
  • Figure 23A shows the illustration of the functional domains of C. difficile toxin A (TcdA), toxin B (TcdB), and binary toxin (CDT) used to construct the chimeric trivalent and quadravalent toxin fusion proteins.
  • TcdA and TcdB share common functional domains including the enzymatic glucosyltransferase (GT) domain, autocatalytic cysteine protease (CP) domain, pore-forming translocation (PT) domain (orange), and receptor binding domain (RBD).
  • GT enzymatic glucosyltransferase
  • CP autocatalytic cysteine protease
  • PT pore-forming translocation
  • RBD receptor binding domain
  • the binary toxin consists of the enzymatic ADP- ribosyltransferase component (CDTa) and receptor binding component (CDTb).
  • CDTb contains a 42 amino acid (aa) signal sequence with two serine-type proteolytic cleavage sites (arrow) which, when cleaved, generates a 20 kDa and 75 kDa fragment.
  • Figure 24B shows the illustration of the chimeric trivalent toxin fusion protein (T-toxin) and a chimeric quadravalent toxin fusion protein (Q-toxin).
  • the T-toxin fusion protein consists of the full-length coding sequence for CDTb with the RBD of TcdB(oo3) containing 24 repeats and the truncated RBD of TcdA with 19 repeats.
  • the expressed T-toxin fusion protein consists of 1813 aa with a molecular weight (MW) of 205 kDa.
  • the Q toxin fusion protein consists of the full-length coding sequence for CDTb to the RBD of TcdB( ⁇ 3) containing 24 repeats, the RBD of TcdA truncated at 19 repeats, and the RBD of TcdB(027) containing 24 repeats.
  • the expressed Q-toxin fusion protein consists of 2359 aa with a molecular weight of 268 kDa.
  • FIGS 24A-24C Expression and Purification of T-Toxin and Q-Toxin Fusion Proteins.
  • SDS-PAGE of purified T-toxin migrates with a molecular weight of 205 kDa and Q-toxin (lanes 4 and 5) migrates with a molecular weight of 268 kDa.
  • Molecular weight marker (lane 1).
  • Figure 24A shows T-toxin and Q-toxin purity was > 90% as determined by SDS-PAGE scanning densitometry.
  • Figure 24B shows western blot analysis as probed with rabbit anti-CDTb specific antibodies.
  • Figure 24C shows western blot analysis as probed with chicken anti-TcdB specific antibodies.
  • Figure 24D shows western blot analysis as probed with chicken anti-TcdA specific antibodies.
  • FIGS 25A-25C Immunogenicity of T-Toxin and Q-Toxin Fusion Proteins in Mice.
  • FIG. 25 A shows serum IgG titers to TcdA, TcdB(003), and CDTb determined by ELISA.
  • Figure 25B shows toxin-neutralizing antibody titers for each toxin determined in the Vero cell assay.
  • FIGS 26A-26D Immunogenicity of T-Toxin and Q-Toxin Fusion Proteins in Hamsters.
  • Two weeks after the third dose samples were collected and analyzed.
  • Figure 26A shows serum IgG titers to TcdA, TcdB(oo3), and CDTb determined by ELISA.
  • Figure 26B shows toxin-neutralizing antibody titers for each toxin determined in the Vero cell assay.
  • adjuvant refers to a compound that, when used in combination with an immunogen, augments or otherwise alters or modifies the immune response induced against the immunogen. Modification of the immune response may include intensification or broadening the specificity of either or both antibody and cellular immune responses.
  • fusion protein means a protein comprised of two or more proteins or protein fragments that are joined or fused, directly or indirectly via a linking peptide, at the amino terminus of one protein and the carboxy terminus of another protein, to form a single continuous polypeptide.
  • a fusion protein may be referred to as a "multivalent protein.”
  • a multivalent protein contains proteins or protein fragments from two or more three discrete protein antigens that are fused together.
  • beneficial or desired results may include inhibiting or suppressing the initiation or progression of an infection or a disease; ameliorating, or reducing the development of, symptoms of an infection or disease; or a combination thereof.
  • prevention is used interchangeably with “prophylaxis” and can mean complete prevention of an infection or disease, or prevention of the development of symptoms of that infection or disease; a delay in the onset of an infection or disease or its symptoms; or a decrease in the severity of a subsequently developed infection or disease or its symptoms.
  • an "effective dose” or “effective amount” refers to an amount of an immunogen sufficient to induce an immune response that reduces at least one symptom of malaria.
  • An effective dose or effective amount may be determined e.g., by measuring amounts of neutralizing secretory and/or serum antibodies, e.g., by plaque neutralization, complement fixation, enzyme-linked immunosorbent (ELISA), or microneutralization assay.
  • ELISA enzyme-linked immunosorbent
  • the term "vaccine” refers to a preparation including an immunogen (e.g. a fusion protein described herein) derived from a pathogen, which is used to induce an immune response against the pathogen that provides protective immunity (e.g., immunity that protects a subject against infection with the pathogen and/or reduces the severity of the disease or condition caused by infection with the pathogen).
  • the protective immune response may include formation of antibodies and/or a cell-mediated response.
  • the term “vaccine” may also refer to a suspension or solution of an immunogen that is administered to a vertebrate to produce protective immunity.
  • the term "subject” includes humans and other animals.
  • the subject in one embodiment, is a human.
  • the term "pharmaceutically acceptable” means being approved by a regulatory agency of the Federal or a state government or listed in the U.S. Pharmacopeia, European Pharmacopeia or other generally recognized pharmacopeia for use in mammals, and more particularly in humans. These compositions can be useful as a vaccine and/or antigenic compositions for inducing a protective immune response in a vertebrate.
  • the present disclosure provides methods and compositions for achieving high expression of large proteins, particularly multivalent proteins containing multiple antigens, from insect cells.
  • the production of high levels of proteins as disclosed herein is particularly unexpected in view of prior experiences in the field.
  • the multivalent (the multivalent protein may also be referred to herein as a multimer) proteins disclosed herein can protect against multiple pathogens and/or the effects from multiple pathogenic proteins from the same organism. For example, certain pathogens may produce multiple molecules that each negatively affects a subject. A more effective response is produced by inducing responses against multiple separate antigens.
  • the proteins multivalent protein contains protein portions from multiple bacterial toxins the In some aspects, the multivalent protein comprises, or consists of, portions of proteins from the same organism, such as toxins for example. In other aspects, the multivalent protein comprises, or consists of, proteins from more than one organism. In particular aspects, no two proteins of a multivalent protein are from the same organism. In some aspects, the same proteins from different strains (i.e., isologs) may be used to produce the portion. Using the same protein from a different strain allows protection against multiple strains and is particularly useful in situations where virulent strains newly arise. Other examples include C. botulinum, which has 8 serological types, A through H.
  • a multimeric protein may contain portions from 2, 3, 4, 5, 6, 7, 8, 9, or 10 different proteins. The portions may be used as components to produce the multimeric immunogenic polypeptides.
  • nucleic acid sequences encoding Q-toxin and BV1512, as well as alternative nucleic acid sequences for B VI 420 and B VI 470, are those using standard codon conversion appropriate degenerate codons that encode the indicated amino acid.
  • Additional vaccine constructs may use the various components above in different orientations.
  • proteins having at least 90% identity to each of these disclosed sequences may be used as components to produce a multimer protein.
  • linkers may be used between one or more proteins in the multivalent proteins.
  • the linker is a poly-(Gly)n linker, wherein n is 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 15, 16, 17, 18, 19, or 20.
  • the linker is GG, GGG, or GGGG (SEQ ID NO: 26).
  • the linker is selected from the group consisting of: dipeptides, tripeptides, and quadripeptides. Preferred dipeptides are Alanine-Serine (AS), Leucine-Glutamic acid (LE), Serine- Arginine (SR).
  • Multivalent antigens are particularly suited for protection against organisms that release multiple toxins into a subject
  • bacteria are known to produce toxins that cause disease in humans.
  • the primary focus of the disclosure is C. difficile; the multimeric polypeptides of the disclosure may be prepared using portions of protein toxins from other species.
  • Toxin-producing species include C. perfringes, C. botulinum, C. difficile, and C. tetani), Bacillus (e.g., B. anthracis), Vibrio (e.g., Vibrio cholerae), Shigella, and Corynebacterium.
  • C. difficile releases two enteric toxins, A and B, which are produced by toxigenic strains.
  • Toxin A is an enterotoxin with minimal cytotoxic activity
  • toxin B is a potent cytotoxin but has limited enterotoxic activity.
  • a third toxin, Binary Toxin, also known as CDT is also produced by the bacteria.
  • Sequences encoding toxin A and B are known (Moncrief et al., Infect. Immun. 65:1105-1108 (1997); Barroso et al., Nucl. Acids Res. 18:4004 (1990); Dove et al. Infect. Immun. 58:480-488 (1990)). Sequences encoding Binary Toxin are also known (Accession Nos. ABS57477, AAB67305, AAF81761).
  • FIG. 1 shows the structure of two exemplary multimer proteins (BV1420 and BV1470). Each multimer contains portions of three toxin proteins, Toxin A (TcdA), Toxin B (TcdB), and binary toxin (CDTb), from C. difficile.
  • Triple toxin 1420 also contains a furin cleavage site. These proteins are large— over 1800 amino acids— and would not be previously have been expected to yield usable amounts of protein when expressed in insect cells. Surprisingly, however, both proteins are expressed at high levels. See Figure 3. Indeed, as Figure 5 demonstrates, the yield for BV1470 was 269 mg/L. Similarly, the yield for BV1420 was 166 mg/L.
  • Quadrivalent toxins are also a preferred type of multimer immunogenic peptide.
  • Figure 20 shows two illustrative examples with four portions or components arranged in sequence. Despite the substantial length of the multimer, good protein production was obtained.
  • Figure 23 illustrates the conversion of a tri-toxin fusion protein to a quadrivalent toxin by addition of portion of a toxin from a second TcdB type. Comparing these two proteins shows that insect cell expression is able to give high level production. See Fig. 24A-D.
  • exemplary multimers include portions organized in various orientation.
  • the first portion may be a TcdA portion, a TcdB portion or a CDTb portion.
  • the second portion may be a TcdA portion, a TcdB portion or a CDTb portion.
  • the third portion may be a TcdA portion, a TcdB portion or a CDTb portion.
  • the fourth portion if present, may be a TcdA portion, a TcdB portion or a CDTb portion.
  • each portion may occupy each position.
  • two adjacent portions are not portions from the same type of toxin.
  • the N-terminal portion is a a CDTb portion.
  • the multivalent proteins disclosed herein are prepared through molecular biology approaches.
  • General texts which describe molecular biological techniques, which are applicable to the present invention, such as cloning, mutation, cell culture and the like, include Berger and Kimmel, Guide to Molecular Cloning Techniques, Methods in Enzymology volume 152 Academic Press, Inc., San Diego, Calif. (Berger); Sambrook et ah, Molecular Cloning—A Laboratory Manual (3rd Ed.), Vol. 1-3, Cold Spring Harbor Laboratory, Cold Spring Harbor, N.Y., 2000 (“Sambrook”) and Current Protocols in Molecular Biology, F. M. Ausubel et al, eds., Current Protocols, a joint venture between Greene Publishing Associates, Inc.
  • the invention also encompasses using known methods of protein engineering and recombinant DNA technology to improve or alter the characteristics of the proteins expressed on or in the fusion proteins of the invention.
  • Various types of mutagenesis can be used to produce and/or isolate variant nucleic acids that encode for protein molecules and/or to further modify/mutate the proteins in or on the fusion proteins of the invention.
  • mutagenesis include but are not limited to site-directed, random point mutagenesis, homologous recombination (DNA shuffling), mutagenesis using uracil containing templates, oligonucleotide-directed mutagenesis, phosphorothioate-modified DNA mutagenesis, mutagenesis using gapped duplex DNA or the like. Additional suitable methods include point mismatch repair, mutagenesis using repair- deficient host strains, restriction-selection and restriction-purification, deletion mutagenesis, mutagenesis by total gene synthesis, double-strand break repair, and the like. Mutagenesis, e.g., involving chimeric constructs, is also included in the present invention. In one embodiment, mutagenesis can be guided by known information of the naturally occurring molecule or altered or mutated naturally occurring molecule, e.g., sequence, sequence comparisons, physical properties, crystal structure or the like.
  • a gene can be cloned as a DNA insert into a vector.
  • vector refers to the means by which a nucleic acid can be propagated and/or transferred between organisms, cells, or cellular components.
  • Vectors include plasmids, viruses, bacteriophages, pro-viruses, phagemids, transposons, artificial chromosomes, and the like, that replicate autonomously or can integrate into a chromosome of a host cell.
  • a vector can also be a naked RNA polynucleotide, a naked DNA polynucleotide, a polynucleotide composed of both DNA and RNA within the same strand, a poly-lysine-conjugated DNA or RNA, a pepti de-conjugated DNA or RNA, a liposome-conjugated DNA, or the like, that is not autonomously replicating.
  • the vectors of the present invention are plasmids or bacmids.
  • the invention comprises nucleotides that encode proteins, including chimeric molecules, cloned into an expression vector that can be expressed in a cell that induces the formation of fusion proteins of the invention.
  • An "expression vector” is a vector, such as a plasmid, that is capable of promoting expression, as well as replication of a nucleic acid incorporated therein.
  • the nucleic acid to be expressed is “operably linked" to a promoter and/or enhancer, and is subject to transcription regulatory control by the promoter and/or enhancer.
  • the nucleotides encode for a Plasmodium protein (as discussed above).
  • the expression vector is a baculovirus vector.
  • proteins may comprise mutations containing alterations which produce silent substitutions, additions, or deletions, e.g., to optimize codon expression for a particular host (change codons in the human mRNA to those preferred by insect cells such as Sf9 cells). See, for example, U.S. Patent Publication 2005/0118191, herein incorporated by reference in its entirety for all purposes.
  • nucleotides can be sequenced to ensure that the correct coding regions were cloned and do not contain any unwanted mutations.
  • the nucleotides can be subcloned into an expression vector (e.g. baculovirus) for expression in any cell.
  • an expression vector e.g. baculovirus
  • the above is only one example of how the proteins can be cloned. A person with skill in the art understands that additional methods may be used.
  • insect cell expression systems include Spodoptera frugiperda (Sf) cells, e.g. Sf9, Sf21, Trichoplusia ni cells, e.g. High Five cells, md Drosophila S2 cells.
  • Sf Spodoptera frugiperda
  • Sf9 Spodoptera frugiperda
  • Sf21 Trichoplusia ni cells
  • Trichoplusia ni cells e.g. High Five cells
  • md Drosophila S2 cells md Drosophila S2 cells.
  • Vectors e.g., vectors comprising polynucleotides that encode fusion proteins
  • vectors can be transfected into host cells according to methods well known in the art
  • introducing nucleic acids into eukaryotic cells can be achieved by calcium phosphate co-precipitation, electroporation, microinjection, lipofection, and transfection employing poly amine transfection reagents.
  • the vector is a recombinant baculovirus.
  • the nanoparticles may be produced by growing host cells transformed by an expression vector under conditions whereby the recombinant proteins are expressed.
  • a method of producing a multivalent protein comprises transfecting vectors encoding the protein into a suitable host cell and expressing the protein under conditions that allow nanoparticle formation.
  • the eukaryotic cell is selected from the group consisting of yeast, insect, amphibian, avian or mammalian cells. The selection of the appropriate growth conditions is within the skill or a person with skill of one of ordinary skill in the art.
  • Methods to grow host cells include, but are not limited to, batch, batch-fed, continuous and perfusion cell culture techniques.
  • Cell culture means the growth and propagation of cells in a bioreactor (a fermentation chamber) where cells propagate and express protein (e.g. recombinant proteins) for purification and isolation.
  • a bioreactor is a chamber used to culture cells in which environmental conditions such as temperature, atmosphere, agitation and/or pH can be monitored.
  • the bioreactor is a stainless steel chamber.
  • the bioreactor is a pre-sterilized plastic bag (e.g. Cellbag®, Wave Biotech, Bridgewater, N. J.). In other embodiment, the pre-sterilized plastic bags are about 50 L to 1000 L bags.
  • the nanoparticles may be harvested from the host cells using detergents.
  • Suitable detergents include non-ionic surfactants.
  • the non-ionic surfactant may be Bis(polyethylene glycol bis[imidazoylcarbonyl]), nonoxynol-9, Bis(polyethylene glycol bis[imidazoyl carbonyl]), Brij® 35, Brij®56, Brij® 72, Brij® 76, Brij® 92V, Brij® 97, Brij® 58P, Cremophor® EL, Decaethyleneglycol monododecyl ether, N-Decanoyl-N- methylglucamine, n-Decyl alpha-Dglucopyranoside,Decyl beta-D-maltopyranoside, n- Dodecanoyl-N-methylglucamide, nDodecyl alpha-D-maltoside, n-Dodecyl beta-D-maltoside, n
  • the cells are isolated from the media and a detergent-containing solution is added to solubilize the cell membrane, releasing the nanoparticles in a detergent extract
  • the detergent may be added to a final concentration of about 0.1% to about 1.0%.
  • the concentration may be about 0.1%, about 0.2%, about 0.3%, about 0.5%, about 0.7%, about 0.8%, or about 1.0 %.
  • the range may be about 0.1% to about 0.3%.
  • the concentration is about 0.2%.
  • the nanoparticles may then be isolated using methods that preserve the integrity thereof, such as centrifugation.
  • centrifugation such as using cesium chloride, sucrose and iodixanol, may be used.
  • Other techniques may be used as alternatives or in addition, such as standard purification techniques including, e.g., ion exchange and gel filtration chromatography.
  • the detergent extract is added to multiple columns sequentially.
  • the first column may be an ion chromatography column, such as TMAE
  • the second column may be a hydrophobic interaction column, such as Phenyl HP
  • the third column may be a strong anion exchange column such as a Source 30Q column. Increased purity may be obtained by repeating the three-step procedure.
  • Production is initiated by seeding Sf9 cells (non-infected) into shaker flasks, allowing the cells to expand and scaling up as the cells grow and multiply (for example from a 125-ml flask to a 50 L Wave bag).
  • the medium used to grow the cell is formulated for the appropriate cell line (preferably serum free media, e.g. insect medium ExCell-420, JRH).
  • the cells are infected with recombinant baculovirus at the most efficient multiplicity of infection (e.g. from about 1 to about 3 plaque forming units per cell).
  • the fusion proteins and, optionally, other immunogens
  • infection is most efficient when the cells are in mid-log phase of growth (4-8 x 10 6 cells/ml) and are at least about 90% viable.
  • Proteins of the disclosure can be harvested approximately 48 to 96 hours post infection. In some aspects, harvesting takes place at about 48 hours, about 72 hours, or between about 48 and about 72 hours. Typically, harvesting takes place when the levels of VLPs in the cell culture medium are near the maximum but before extensive cell lysis.
  • the Sf9 cell density and viability at the time of harvest can be about 0.5 xlO 6 cells/ml to about 1.5 xlO 6 cells/ml with at least 20% viability, as shown by dye exclusion assay.
  • the eluate is appled to Phenyl HP columns (Buffer A: 350 mM Na-Citrate/25 mM Tris pH7.5 and Buffer B: 5 mM Tris pH8.0) and then to a Source 30Q column (Buffer A: 25 mM Tris pH8.0/250 mM NaCl Buffer B: 25 mM Tris pH8.0/lM NaCl).
  • Phenyl HP columns Buffer A: 350 mM Na-Citrate/25 mM Tris pH7.5 and Buffer B: 5 mM Tris pH8.0
  • Buffer A 25 mM Tris pH8.0/250 mM NaCl
  • Buffer B 25 mM Tris pH8.0/lM NaCl
  • the procedures described above enable a purity of at least about 90%, at least about 95% or about 98% at a yield of 150 mg/L to about 300 mg/L. Purity may be measured by gel-based approaches that indicate total protein.
  • the intact baculovirus can be inactivated, if desired. Inactivation can be accomplished by chemical methods, for example, formalin or ⁇ -propiolactone (BPL). Removal and/or inactivation of intact baculovirus can also be largely accomplished by using selective precipitation and chromatographic methods known in the art, as exemplified above. Methods of inactivation comprise incubating the sample containing the VLPs in 0.2% of BPL for 3 hours at about 25 °C to about 27 °C. The baculovirus can also be inactivated by incubating the sample containing the VLPs at 0.05% BPL at 4 °C for 3 days, then at 37 °C for one hour.
  • the above techniques can be practiced across a variety of scales. For example, T-flasks, shake-flasks, spinner bottles, up to industrial sized bioreactors.
  • the bioreactors can comprise either a stainless steel tank or a pre-sterilized plastic bag (for example, the system sold by Wave Biotech, Bridgewater, N.J.). A person with skill in the art will know what is most desirable for the particular circumstance.
  • the yield for the multimer proteins using the methods disclosed herein is remarkable.
  • the yield is about 150 mg/L to about 300 mg/L.
  • the yield is about 40 mg/L, about 60 mg/L, about 80 mg/L, about 100 mg/L, about 150 mg/L, about 200 mg/L, about 250 mg/L, or about 300 mg/L.
  • the yield ranges from about 40 mg/L to about 300 mg/L, from about 80 mg/L to about 250 mg/L, or about 100 mg/mL to about 300 mg/L.
  • Large multimer proteins disclosed herein typically range from about 1500-2500 amino acids. In some aspects, they range from about 1500 to about 2000 amino acids. In other aspects, they range from about 1800 to about 2000 amino acids.
  • the multimer proteins form nanoparticles having a typical diameter of about 11 nm to about 35 nm.
  • the diameter range may be about 15 nm to about 25 nm.
  • Illustrative examples of multimer protein nanoparticles in these ranges are shown in Figure 9.
  • the purified multimer protein may be about 80% soluble, about 85% soluble, about 90% soluble, about 95% soluble, about 97% soluble, or about 99% soluble. In some aspects, solubility is about 90% to about 99% or about 90% to about 95%.
  • the antigens disclosed herein encompass variations and mutants of those antigens.
  • the antigen may share identity to a disclosed antigen.
  • the percentage identity may be at least 80%, at least 90%, at least 95%, at least 97%, or at least 98%. Percentage identity can be calculated using the alignment program Clustal Omega, available at www.ebi.ac.uk/Tools/msa/clustalo using default parameters.
  • the protein contained in the nanoparticles consists of that protein.
  • the protein contained in the nanoparticles comprise that protein. Extensions to the protein itself may be for various purposes.
  • the antigen may be extended at the N-terminus, the C-terminus, or both.
  • the extension is a tag useful for a function, such as purification or detection.
  • the tag contains an epitope.
  • the tag may be a polyglutamate tag, a FLAG-tag, a HA-tag, a polyHis-tag (having about 5-10 histidines), a Myc-tag, a Glutathione-S- transferase-tag, a Green fluorescent protein-tag, Maltose binding protein-tag, a Thioredoxin-tag, or an Fc-tag.
  • the extension may be an N-terminal signal peptide fused to the protein to enhance expression. While such signal peptides are often cleaved during expression in the cell, some nanoparticles may contain the antigen with an intact signal peptide. Thus, when a nanoparticle comprises an antigen, the antigen may contain an extension and thus may be a fusion protein when incorporated into nanoparticles. For the purposes of calculating identity to the sequence, extensions are not included.
  • the antigen may be truncated.
  • the N-terminus may be truncated by about 10 amino acids, about 30 amino acids, about 50 amino acids, about 75 amino acids, about 100 amino acids, or about 200 amino acids.
  • the C-terminus may be truncated by about 10 amino acids, about 30 amino acids, about 50 amino acids, about 75 amino acids, about 100 amino acids, or about 200 amino acids.
  • compositions disclosed herein comprise a multimer protein and a pharmaceutically acceptable carrier.
  • Pharmaceutically acceptable carriers include any pharmaceutical agent that can be administered to a subject without undue toxicity, irritation, or allergic reaction.
  • Pharmaceutically acceptable carriers may also include one or more pharmaceutically acceptable excipient
  • a pharmaceutically acceptable excipient is any excipient that is useful in preparing a pharmaceutical composition that is generally safe and non-toxic, and is acceptable for veterinary as well as human pharmaceutical use.
  • compositions useful herein contain a pharmaceutically acceptable carrier, including any suitable diluent or excipient, which includes any pharmaceutical agent that does not itself induce the production of an immune response harmful to the vertebrate receiving the composition, and which may be administered without undue toxicity and an immunogen; for example a multimer fusion protein.
  • a pharmaceutically acceptable carrier including any suitable diluent or excipient, which includes any pharmaceutical agent that does not itself induce the production of an immune response harmful to the vertebrate receiving the composition, and which may be administered without undue toxicity and an immunogen; for example a multimer fusion protein.
  • formulations may include a pharmaceutically acceptable carrier or excipient.
  • Pharmaceutically acceptable carriers include but are not limited to saline, buffered saline, dextrose, water, glycerol, sterile isotonic aqueous buffer, and combinations thereof.
  • the formulation may be adapted to suit the mode of administration.
  • the formulation is suitable for administration to humans, is sterile, non-particulate and/or non- pyrogenic.
  • the composition may also contain wetting agents, or emulsifying agents, or pH buffering agents, or mixtures thereof.
  • the composition can be a solid form, such as a lyophilized powder suitable for reconstitution (e.g., with water or saline), a liquid solution, suspension, emulsion, tablet, pill, capsule, sustained release formulation, or powder.
  • Oral formulations may include standard carriers such as pharmaceutical grades of mannitol, lactose, starch, magnesium stearate, sodium saccharine, cellulose, magnesium carbonate, etc.
  • the immunogenicity of a particular composition may be enhanced by the use of nonspecific stimulators of the immune response, known as adjuvants.
  • adjuvants have been used experimentally to promote a generalized increase in immunity against antigens (e.g., U.S. Pat. No. 4,877,611). Immunization protocols have used adjuvants to stimulate responses for many years, and as such, adjuvants are well known to one of ordinary skill in the art. Some adjuvants affect the way in which antigens are presented. For example, the immune response is increased when protein antigens are precipitated by alum. Emulsification of antigens also prolongs the duration of antigen presentation.
  • the inclusion of any adjuvant described in Vogel et al., "A Compendium of Vaccine Adjuvants and Excipients (2nd Edition)," herein incorporated by reference in its entirety for all purposes, is envisioned within the scope of this disclosure.
  • Exemplary adjuvants include complete Freund's adjuvant (a non-specific stimulator of the immune response containing killed Mycobacterium tuberculosis), incomplete Freund's adjuvants and aluminum hydroxide adjuvant.
  • Other adjuvants comprise GMCSP, BCG, MDP compounds, such as thur-MDP and nor-MDP, CGP (MTP-PE), lipid A, and monophosphoryl lipid A (MPL), MF-59, RIBI, which contains three components extracted from bacteria, MPL, trehalose dimycolate (TDM) and cell wall skeleton (CWS) in a 2% squalene/Tween® 80 emulsion.
  • the adjuvant may be a paucilamellar lipid vesicle; for example, Novasomes®.
  • Novasomes® are paucilamellar nonphospholipid vesicles ranging from about 100 nm to about 500 nm. They comprise Brij 72, cholesterol, oleic acid and squalene. Novasomes have been shown to be an effective adjuvant (see, U.S. Pat. Nos. 5,629,021, 6,387,373, and 4,911,928.
  • Adjuvants containing saponin may also be combined with the immunogens disclosed herein.
  • Saponins are glycosides derived from the bark of the Quillaja saponaria Molina tree. Typically, saponin is prepared using a multi-step purification process resulting in multiple fractions.
  • saponin fraction from Quillaja saponaria Molina is used genetically to describe a semi-purified or defined saponin fraction of Quillaja saponaria or a substantially pure fraction thereof.
  • Fractions A, B, and C are described in U.S. Pat. No. 6,352,697 and may be prepared as follows.
  • a lipophilic fraction from Quil A a crude aqueous Quillaja saponaria Molina extract, is separated by chromatography and eluted with 70% acetonitrile in water to recover the lipophilic fraction.
  • This lipophilic fraction is then separated by semi-preparative HPLC with elution using a gradient of from 25% to 60% acetonitrile in acidic water.
  • Fraction A Fraction A or “QH-A” is, or corresponds to, the fraction, which is eluted at approximately 39% acetonitrile.
  • Fraction B Fraction B or “QH-B” is, or corresponds to, the fraction, which is eluted at approximately 47% acetonitrile.
  • Fraction C Fraction C or “QH-C” is, or corresponds to, the fraction, which is eluted at approximately 49% acetonitrile. Additional information regarding purification of Fractions is found in U.S Pat No. 5,057,540.
  • Fractions A, B and C of Quillaja saponaria Molina each represent groups or families of chemically closely related molecules with definable properties.
  • the chromatographic conditions under which they are obtained are such that the batch-to-batch reproducibility in terms of elution profile and biological activity is highly consistent.
  • Fractions B3, B4 and B4b are described in EP 0436620.
  • Fractions QA1-QA22 are described EP03632279 B2, Q-VAC (Nor-Feed, AS Denmark), Quillaja saponaria Molina Spikoside (lsconova AB, Ultunaallen 2B, 756 51 Uppsala, Sweden).
  • the saponin fractions described herein and used for forming adjuvants are often substantially pure fractions; that is, the fractions are substantially free of the presence of contamination from other materials.
  • a substantially pure saponin fraction may contain up to 40% by weight, up to 30% by weight, up to 25% by weight, up to 20% by weight, up to 15% by weight, up to 10% by weight, up to 7% by weight, up to 5% by weight, up to 2% by weight, up to 1% by weight, up to 0.5% by weight, or up to 0.1% by weight of other compounds such as other saponins or other adjuvant materials.
  • Saponin fractions may be administered in the form of a cage-like particle referred to as an ISCOM (Immune Stimulating COMplexY ISCOMs may be prepared as described in EP0109942B1, EP0242380B1 and EP0180546 Bl.
  • a transport and/or a passenger antigen may be used, as described in EP 9600647-3 (PCT/SE97/00289).
  • the ISCOM is an ISCOM matrix complex.
  • An ISCOM matrix complex comprises at least one saponin fraction and a lipid.
  • the lipid is at least a sterol, such as cholesterol.
  • the ISCOM matrix complex also contains a phospholipid.
  • the ISCOM matrix complexes may also contain one or more other immunomodulatory (adjuvant- active) substances, not necessarily a glycoside, and may be produced as described in EP0436620B1.
  • the ISCOM is an ISCOM complex.
  • An ISCOM complex contains at least one saponin, at least one lipid, and at least one kind of antigen or epitope.
  • the ISCOM complex contains antigen associated by detergent treatment such that that a portion of the antigen integrates into the particle.
  • ISCOM matrix is formulated as an admixture with antigen and the association between ISCOM matrix particles and antigen is mediated by electrostatic and/or hydrophobic interactions.
  • the saponin fraction integrated into an ISCOM matrix complex or an ISCOM complex, or at least one additional adjuvant, which also is integrated into the ISCOM or ISCOM matrix complex or mixed therewith is selected from fraction A, fraction B, or fraction C of Quillaja saponaria, a semipurified preparation of Quillaja saponaria, a purified preparation of Quillaja saponaria, or any purified sub-fraction e.g., QA 1-21.
  • each ISCOM particle may contain at least two saponin fractions. Any combinations of weight % of different saponin fractions may be used. Any combination of weight % of any two fractions may be used.
  • the particle may contain any weight % of fraction A and any weight % of another saponin fraction, such as a crude saponin fraction or fraction C, respectively.
  • each ISCOM matrix particle or each ISCOM complex particle may contain from 0.1 to 99.9 by weight, 5 to 95% by weight, 10 to 90% by weight 15 to 85% by weight, 20 to 80% by weight, 25 to 75% by weight, 30 to 70% by weight, 35 to 65% by weight, 40 to 60% by weight, 45 to 55% by weight, 40 to 60% by weight, or 50% by weight of one saponin fraction, e.g. fraction A and the rest up to 100% in each case of another saponin e.g. any crude fraction or any other faction e.g. fraction C. The weight is calculated as the total weight of the saponin fractions.
  • Examples of ISCOM matrix complex and ISCOM complex adjuvants are disclosed in U.S Published Application No. 2013/0129770.
  • the ISCOM matrix or ISCOM complex comprises from 5- 99% by weight of one fraction, e.g. fraction A and the rest up to 100% of weight of another fraction e.g. a crude saponin fraction or fraction C. The weight is calculated as the total weight of the saponin fractions.
  • the ISCOM matrix or ISCOM complex comprises from 40% to 99% by weight of one fraction, e.g. fraction A and from 1% to 60% by weight of another fraction, e.g. a crude saponin fraction or fraction C. The weight is calculated as the total weight of the saponin fractions.
  • the ISCOM matrix or ISCOM complex comprises from 70% to 95% by weight of one fraction e.g., fraction A, and from 30% to 5% by weight of another fraction, e.g., a crude saponin fraction, or fraction C. The weight is calculated as the total weight of the saponin fractions.
  • the saponin fraction from Quillaja saponaria Molina is selected from any one of QA 1-21.
  • ISCOM matrix particles and ISCOM complex particles may each be formed using only one saponin fraction.
  • Compositions disclosed herein may contain multiple particles wherein each particle contains only one saponin fraction. That is, certain compositions may contain one or more different types of ISCOM-matrix complexes particles and/or one or more different types of ISCOM complexes particles, where each individual particle contains one saponin fraction from Quillaja saponaria Molina, wherein the saponin fraction in one complex is different from the saponin fraction in the other complex particles.
  • one type of saponin fraction or a crude saponin fraction may be integrated into one ISCOM matrix complex or particle and another type of substantially pure saponin fraction, or a crude saponin fraction, may be integrated into another ISCOM matrix complex or particle.
  • a composition or vaccine may comprise at least two types of complexes or particles each type having one type of saponins integrated into physically different particles.
  • mixtures of ISCOM matrix complex particles and/or ISCOM complex particles may be used in which one saponin fraction Quillaja saponaria Molina and another saponin fraction Quillaja saponaria Molina are separately incorporated into different ISCOM matrix complex particles and/or ISCOM complex particles.
  • the ISCOM matrix or ISCOM complex particles which each have one saponin fraction, may be present in composition at any combination of weight %.
  • a composition may contain 0.1% to 99.9% by weight, 5% to 95% by weight, 10% to 90% by weight, 15% to 85% by weight, 20% to 80% by weight, 25% to 75% by weight, 30% to 70% by weight, 35% to 65% by weight, 40% to 60% by weight, 45% to 55% by weight, 40 to 60% by weight, or 50% by weight, of an ISCOM matrix or complex containing a first saponin fraction with the remaining portion made up by an ISCOM matrix or complex containing a different saponin fraction.
  • the remaining portion is one or more ISCOM matrix or complexes where each matrix or complex particle contains only one saponin fraction.
  • the ISCOM matrix or complex particles may contain more than one saponin fraction.
  • the saponin fraction in a first ISCOM matrix is Fraction A (a "Fraction A Matrix") and the saponin fraction in a second ISCOM matrix or ISCOM complex particle is Fraction C (a "Fraction C Matrix").
  • preferred compositions comprise, as an adjuvant, a Fraction A Matrix adjuvant and a Fraction C Matrix adjuvant.
  • the amounts of each Matrix in the composition may vary.
  • the amount of Fraction A Matrix may be about 80% (w/w), about 85% (w/w), about 90% (w/w), about 92% (w/w), or about 95% (w/w) with the remainder Fraction C Matrix.
  • a suitable example of a suitable 85:15 Fraction A Matrix and Fraction C Matrix combination is Matrix-MTM (Novavax AB, Uppsala, Sweden), a mixture of Fraction A Matrix and Fraction C Matrix at a ratio of about 85 to about 15.
  • compositions of the disclosure may also be formulated with "immune stimulators.” These are the body's own chemical messengers (cytokines) to increase the immune system's response. Immune stimulators include, but are not limited to, various cytokines, lymphokines and chemokines with immunostimulatory, immunopotentiating, and pro-inflammatory activities, such as interleukins (e.g., IL-1, IL-2, IL-3, IL-4, IL-12, IL-13); growth factors (e.g., granulocyte- macrophage (GM)-colony stimulating factor (CM); and other immunostimulatory molecules, such as macrophage inflammatory factor, Flt3 ligand, B7.1 ; B7.2, etc.
  • interleukins e.g., IL-1, IL-2, IL-3, IL-4, IL-12, IL-13
  • growth factors e.g., granulocyte- macrophage (GM)-colony stimulating factor (CM)
  • CM colonn
  • the immunostimulatory molecules may be administered in the same formulation as the compositions of the disclosure, or may be administered separately. Either the protein or an expression vector encoding the protein may be administered to produce an immunostimulatory effect.
  • the disclosure comprises antigenic and vaccine formulations comprising an adjuvant and/or an immune stimulator.
  • Also provided in the present disclosure are methods of eliciting an immune response against pathogens.
  • the method involves administering an immunologically effective amount of a composition comprising a multimer protein to a subject
  • Administration of an immunologically effective amount of the composition of the disclosure elicits an immune response specific for epitopes present on the fusion protein.
  • an immune response can include B cell responses and/or T cell responses.
  • the multimer proteins preferably induce neutralizing antibodies.
  • the immune response includes elements that are specific for at least one conformational epitope present each protein contained in the multimer protein.
  • Administration may be by any suitable route. Suitable routes include parenteral administration (e.g., intradermal, intramuscular, intravenous and subcutaneous), epidural, and mucosal (e.g., intranasal and oral or pulmonary routes or by suppositories), transdermally or intradermally. Administration may be by infusion or bolus injection, by absorption through epithelial or mucocutaneous linings (e.g., oral mucous, colon, conjunctiva, nasopharynx, oropharynx, vagina, urethra, urinary bladder and intestinal mucosa, etc.) and may be administered together with other biologically active agents. In some aspects, intranasal or other mucosal routes of administration may result in an antibody or other immune response that is substantially higher than other routes of administration. Administration can be systemic or local.
  • parenteral administration e.g., intradermal, intramuscular, intravenous and subcutaneous
  • epidural e.
  • administration may be by injection using a needle and syringe, by a needle-less injection device.
  • administration is by drops, large particle aerosol (greater than about 10 microns), or by spray into the upper respiratory tract.
  • a pharmaceutical pack or kit comprising one or more containers filled with one or more of the components of the formulations.
  • the kit may include two containers, a first container containing a multimer protein, and a second container containing an adjuvant.
  • Associated with such container(s) may be a notice in the form prescribed by a governmental agency regulating the manufacture, use or sale of pharmaceuticals or biological products, which notice reflects approval by the agency of manufacture, use or sale for human administration.
  • Formulations may also be packaged in a hermetically sealed container such as an ampoule or sachette indicating the quantity of composition.
  • administration may be targeted.
  • the compositions may be administered in such a manner as to target mucosal tissues in order to elicit an immune response at the site of immunization.
  • Mucosal tissues such as gut associated lymphoid tissue (GALT) can be targeted for immunization by using oral administration of compositions which contain adjuvants with particular mucosal targeting properties.
  • Additional mucosal tissues can also be targeted, such as nasopharyngeal lymphoid tissue (NALT) and bronchial-associated lymphoid tissue (BALT).
  • compositions may be administered each having different collections of antigens.
  • the proteins may be co-administered simultaneously to the same position of the subject; for example, by injection of material from one or more containers containing multimer proteins.
  • they may be co-administered sequentially at different sites within a short space of time; for example, one administration may be in the thigh, and a second administration may be in the arm, with both administrations occurring within a short period (e.g. up to 30 minutes).
  • While stimulation of immunity with a single dose is possible, additional dosages may be administered, by the same or different route, to achieve the desired effect.
  • multiple administrations may be required to elicit sufficient levels of immunity.
  • Administration can continue at intervals throughout childhood, as necessary to maintain sufficient levels of protection against infections.
  • adults who are particularly susceptible to repeated or serious infections such as, for example, health care workers, day care workers, family members of young children, the elderly, and individuals with compromised cardiopulmonary function may require multiple immunizations to establish and/or maintain protective immune responses.
  • Levels of induced immunity can be monitored, for example, by measuring amounts of neutralizing secretory and serum antibodies, and dosages adjusted or vaccinations repeated as necessary to elicit and maintain desired levels of protection.
  • the vaccine compositions may also be used for preparing antibodies against the toxins useful for passive administration therapies. See Casadevall. "Passive Antibody Administration (Immediate Immunity) as a Specific Defense against Biological Weapons,” Emerging Infectious Diseases. 2002;8(8):833-841.
  • Triple toxin 1420 (also referred to as BV1420) contains, from N-terminus to C- terminus, an Activation domain peptide, a mature CDTb peptide, a TcdB RBD peptide, and a TcdA RBD peptide containing 19 repeats (R19).
  • a furin cleavage site (RARRRKKR; SEQ ID NO:27) was located between the activation domain and mature CDTb peptides.
  • Figures 2 and 3 show the protein and genetic sequence of BV1470, respectively. Linker sites at either end of the TcdB peptide.
  • Sf9 cells were transformed with a baculovirus vector expressing the triple vaccine as a single transcript.
  • Expression data from the Sf9 cells is shown in Figure 2.
  • Figure 2 shows expression of each proteins harvested at 48 hours and at 72 hours. Remarkably, even though each protein is over 200kDa, high level production is achieved.
  • Figure 7 shows a time course of expression from 48 hours to 96 hours. The data shows that, for both proteins, the protein is highly soluble.
  • Tergitol was directly added to cell culture to final concentration of 0.2% NP9/25 mM Tris/50 mM NaCl/pH8.0. Incubate at room temperature for 1 hour then centrifuge the lysate at 9000 g for 30 min twice. Collected the supernatant containing the nanoparticles. The supernatant is then added to in Buffer A and eluted in Buffer B (Buffer A: 25mM Tris pH 8.0 /50 mM NaCl Buffer B: 25 mM Tris pH 8.0/1M NaCl).
  • the eluate is appled to Phenyl HP columns (Buffer A: 350 mM Na-Citrate/25 mM Tris pH7.5 and Buffer B: 5 mM Tris pH8.0) and then to a Source 30Q column (Buffer A: 25 mM Tris pH8.0/250 mM NaCl Buffer B: 25 mM Tris pH8.0/lM NaCl).
  • the pooled fractions containing the product are passed through a 2 micron filter. See Figures 4-6. Purification of 1470 from Sf9 yielded 269 mg/liter of protein. Purification of 1420 from Sf9 cells yielded 166 mg/liter.
  • Particle size distribution by volume graph for triple toxin BV1420 was analyzed by dynamic light scattering using a Zeta Sizer Nano. Graph of size distribution by volume is shown in Figure 7. The average diameter was -30 nm. Figure 8 shows particle size distribution by intensity graph for triple toxin BV1470. The average diameter was ⁇ 18 nm.
  • Figure 9 shows various electronmicrographs of negative stained triple toxin BV1420. Electron-micrograph of purified triple toxin B VI 420 was diluted to approximately lOug/ml and negatively stained with uranyl acetate.
  • Figure 10 provides the results of a mouse trial of the Triple Toxin Vaccine against Toxin A and Binary Toxin.
  • Groups 1-6 were administered BV1420 antigen (30 ⁇ g) or PBS as shown.
  • Groups 1 and 4 contain 50 ⁇ g Alum OH;
  • Groups 2 and 5 contained 50 ⁇ g Alum OH and 50 ⁇ g ISCOM Matrix M adjuvant.
  • Mice were immunized at Day 0 and Day 14, with bleeds at Day 0, 14, and 32. Mice were challenged with Toxin A or Binary Toxin at Day 35.
  • FIG 11 shows serum IgG responses. PBS did not induce antibodies, as expected.
  • Figure 12 establishes that the antibodies neutralized both Toxin A and CTDb.
  • Figure 13 shows animal survival for the 6 groups. Groups 1, 2, 4, and 5 showed 100% survival. Except for two mice in the binary toxin challenge, all the animals in the control PBS groups died. These data establish that the triple toxin vaccine protects against the effect of the toxins.
  • mice were administered BV1420 (30 ⁇ g) with Alum OH.
  • Group 2 mice were administered BV1470 (30 ⁇ g) with Alum OH,
  • Group 3 was administered a tandem protein containing rotavirus VP6 and the TcdB RBD (10 ⁇ g) with Alum OH.
  • Group 4 mice were administered BV1470 and VP6/TcdB RBD.
  • Group 5 was administered Toxoid B (10 ⁇ g).
  • Group 6 was the control and was administered PBS.
  • Anti-IgG response is shown in Figure IS. High titers antibodies were obtained in each case.
  • Each of the groups containing the Toxin A peptide induced high titer anti-Toxin A responses ranging between 10 4 and about 10 5 . All groups were administered the Toxin B peptide and each demonstrated high titer ranging between 10 4 and about 10 6 . Each of the groups containing the Binary Toxin peptide induced high titer responses ranging between 10 s and about 10 6 .
  • Figure 16 establishes that the antibodies were produced that neutralized both Toxin B, with the Toxoid B showing higher levels.
  • FIG. 18 and 19 shows additional trivalent vaccine proteins with the TcdB gene translocations gene.
  • BV1S12 is shown in the bottom diagram.
  • Figures 18 shows additional vaccines structures: Multimer Protein Sequence: Sequence of BV1512 multimer vaccine protein showing CDTb protein separated from the Translocation Domain (TD) by an A-S linker and the TD separated from the TcdAR19 portion by an S-R linker.
  • Figure 19 shows expression of the multimer protein BV1512 from Sf9 cells.
  • Multimer proteins containing four peptides were produced.
  • Fig. 20 In this example, a peptide from a second TcdB strain was introduced to broaden immunity against an additional C. difficile strain.
  • the first quadrivalent multimer protein (CBAB, or pCDTb/TcdB63o TcdAR19/TcdBo27) included a TcdB peptide from Strain 027 added at the C- terminus (See Fig. 20, upper diagram).
  • a TcdB peptide from Strain 027 peptide was introduced between the TcdB protein and the TcdA(R19) protein from the first strain, strain 630 (See Fig. 20, lower diagram).
  • Figure 21 shows expression of the CBBA quadrivalent multimer from Sf9 cells as described above. The data shows that the yield obtained was 42 mg/L.
  • a second protein (CBBA, or pCDTb/TTcdB63o,TcdARl 9/TcdBo27 as shown in Figure 26) was also produced in the Sf9 system and achieved 40 mg/L yield. See Fig. 22.
  • Chimeric fusion proteins were constructed to encode RBD of C. difficile TcdA, TcdB(oo3), TcdB(027), and CDTb.
  • the RBD amino acid sequence for TcdA was derived from C. difficile strain VPI 10463 (ATCC 43255), NCBI P16154 (toxinotype 0, ribotype 003); TcdB «x)3) from strain VPI 10463 (ATCC 43255), NCBI PI 8177 (toxinotype 0, ribotype 003); TcdB ⁇ from strain CD196, NCBI WP_009888442.1 (toxinotype m, ribotype 027); and CDTb from strain CD196, GenBank ABS57477.1 (toxinotype III, ribotype 027).
  • TcdA RBD truncated with 19 of 38 repeats
  • TcdB «x)3
  • TcdB(027) RBDs 24 repeats each
  • CDTb CDTb
  • the nucleotide sequences encoding the CDTb gene fragment (amino acids 1-835), TcdA RBD (1314 base pairs [bp], 6816-8130 bp), and TcdB(0O3) RBD (1608 bp, 5493-7098 bp) were obtained by PCR amplification from the synthesized gene. PCR-amplified gene fragments were digested with restriction enzyme: CDTb with BamHI Nhel; TcdB(0O3) RBD with Nhel/Xbal; and TcdA RBD with Xbal/Hindlll.
  • TcdB(027) RBD (1608 bp, 5493-7098) digested with Spel/ ⁇ was fused to the C- terminus of the trivalent fusion gene to form the plasmid and baculovirus construct encoding the RBD of all four toxins, which was similarly expressed in Sf9 cells to produce the quadravalent fusion protein, hereafter referred to as Q-toxin ( Figure 23B; SEQ ID NO: 21).
  • Each of the portion is separated by a two amino acid linker: AS between the pCDTb portion and the TcdB003 portion, SR between the TcdB003 portion and the TcdA portion, TS between the TcdA portion and the TcdB027 portion.
  • Fusion proteins were extracted by detergent lysis in a buffer comprising 0.2% Tergitol NP-9 in 25 inM Tris buffer (pH 8.0), 250 inM NaCl and 2 ⁇ g/mL leupeptin. Lysates were purified by centrifugation, and the fusion proteins were purified with Fractogel EMD TMAE, phenyl HP and 30Q column chromatography. Purified T-toxin and Q-toxin were formulated in 25 inM Tris and 250 inM NaCl (pH 8.0) at approximately 4.0 mg/mL and stored at ⁇ -60°C. Recovery of purified T-toxin and Q-toxin was 267 and 154 mg/L, respectively.
  • T-toxin and Q- toxin migrate in SDS-PAGE gels with molecular weights of 205 kDa and 268 kDa, respectively, and purity of > 90% (Figure 23A).
  • Western blot analysis with toxin-specific antibodies confirmed expression of CDTb, TcdB, and TcdA in each fusion protein ( Figure 23B-D).
  • T-toxin and Q-toxin Fusion Proteins were assessed for immunogenicity of T-toxin and Q-toxin Fusion proteins.
  • Mouse studies were conducted in accordance with Noble Life Sciences' Institutional Animal Care and Use Committee (IACUC) approved protocols.
  • Female C57BL/6 mice (6-8 weeks old) were immunized IM on Days 0 and 14 with T-toxin (30 or 100 ⁇ g) or Q-toxin (100 ⁇ g) formulated with SO ⁇ g aluminum hydroxide (alum), or PBS (control). Serum was collected 18 days after the second dose.
  • Mice were challenged intraperitoneally (IP) 3 weeks after the second immunization with a 100% minimal lethal dose (MLDioo%) of TcdA, TcdB(oo3), or CDTa and CDTb.
  • IP intraperitoneally
  • MLDioo% 100% minimal lethal dose
  • Titers were reported as the reciprocal dilution that resulted in a reading of 50% the maximum OD4sonm. Titer values recorded as below the lower limit of detection (LLOD) were assigned a titer 50 for calculating GMT. Mouse serum IgG titers following immunization were high for TcdA, TcdB, and CDT and comparable between T-toxin and Q-toxin (Figure 25 A).
  • Vero cells CCL-81, ATCC
  • FBS heat-inactivated fetal bovine serum
  • Gibco antibiotics
  • assay medium lx DMEM with 5% heat-inactivated FBS, lx NEAA, 0.3% dextrose, lx penicillin/streptomycin/glutamine, 0.006% Phenol Red
  • Vero cells 7.5 x 10 4 cells/mL suspended in 50 ⁇ . medium and 150 sterile mineral oil (Sigma) were added and plates were incubated for 6-7 days at 37°C. After incubation, plates were observed for well color.
  • mice were challenged TcdB(oo3).
  • Vero cells CCL-81, ATCC
  • FBS heat-inactivated fetal bovine serum
  • Gibco antibiotics
  • Two-fold serial dilutions of hamster sera were prepared in 96-well, flat-bottom tissue culture plates (Thermo Scientific).
  • assay medium lx DMEM with 5% heat-inactivated FBS, lx NEAA, 0.3% dextrose, lx penicillin/streptomycin/glutamine, 0.006% Phenol Red
  • Vera cells 7.5 x 10 4 cells/mL suspended in 50 ⁇ . medium and 150 uL sterile mineral oil (Sigma) were added and plates were incubated for 6-7 days at 37°C. After incubation, plates were observed for well color.

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CN201880025192.8A CN110691609B (zh) 2017-03-15 2018-03-15 用于诱导针对艰难梭菌的免疫应答的方法和组合物
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JP2019550687A JP7149285B2 (ja) 2017-03-15 2018-03-15 Ｃｌｏｓｔｒｉｄｉｕｍ ｄｉｆｆｉｃｉｌｅに対する免疫応答を誘導するための方法および組成物
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IL269258A IL269258B2 (en) 2017-03-15 2018-03-15 Methods and compositions for inducing immune responses against Clostridium difficile
US16/494,517 US11123419B2 (en) 2017-03-15 2018-03-15 Methods and compositions for inducing immune responses against Clostridium difficile
RU2019132111A RU2781057C9 (ru) 2017-03-15 2018-03-15 Способы и композиции для индукции иммунного ответа против clostridium difficile
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US11535652B2 (en) 2011-04-22 2022-12-27 Wyeth Llc Compositions relating to a mutant clostridium difficile toxin and methods thereof
WO2023232901A1 (en) 2022-06-01 2023-12-07 Valneva Austria Gmbh Clostridium difficile vaccine
US11952597B2 (en) 2012-10-21 2024-04-09 Pfizer Inc. Compositions and methods relating to a mutant Clostridium difficile toxin

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MX2019010948A (es) * 2017-03-15 2020-01-09 Novavax Inc Métodos y composiciones para inducir respuestas inmunitarias contra clostridium difficile.

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MX2019010948A (es) 2017-03-15 2020-01-09 Novavax Inc Métodos y composiciones para inducir respuestas inmunitarias contra clostridium difficile.

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US11535652B2 (en) 2011-04-22 2022-12-27 Wyeth Llc Compositions relating to a mutant clostridium difficile toxin and methods thereof
US11952597B2 (en) 2012-10-21 2024-04-09 Pfizer Inc. Compositions and methods relating to a mutant Clostridium difficile toxin
WO2021255690A3 (en) * 2020-06-19 2022-02-10 Pfizer Inc. Immunogenic compositions against clostridioides (clostridium) difficile and methods thereof
WO2023232901A1 (en) 2022-06-01 2023-12-07 Valneva Austria Gmbh Clostridium difficile vaccine

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